Evidence map›Paper›PMID 32772515›Full record

ArticleJournal of clinical research in pediatric endocrinology2021

A Case of Congenital Central Hypothyroidism Caused by a Novel Variant (Gln1255Ter) in

Doğa Türkkahraman, Nimet Karataş Torun, Nadide Cemre Randa

Open access · goldAbstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in Journal of clinical research in pediatric endocrinology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 40% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Identification of a Novel Nonsense Mutation in theChildren (Basel, Switzerland) · 2025
    Article
  2. A Novel Pathogenic IGSF1 Variant in a Patient with GH and TSH Deficiency Diagnosed by HighJournal of clinical research in pediatric endocrinology · 2023
    Article
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors at 1 institution in 1 country.

Doğa TürkkahramanUniversity of Health Sciences Turkey, Antalya Training and Research Hospital, Clinic of Pediatric Endocrinology, Antalya, TurkeyORCID 0000-0002-7472-5712
Nimet Karataş TorunUniversity of Healty Sciences Turkey, Antalya Training and Research Hospital, Clinic of Pediatrics, Antalya, TurkeyORCID 0000-0002-0120-8845
Nadide Cemre RandaUniversity of Healty Sciences Turkey, Antalya Training and Research Hospital, Clinic of Medical Genetics, Antalya, TurkeyORCID 0000-0002-0917-2787
Antalya Eğitim ve Araştırma Hastanesi · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Loss-of-function mutations in the

Indexed as

Codon, NonsenseChildCongenital HypothyroidismDNA Mutational AnalysisGenetic Predisposition to DiseaseHemizygoteHumansImmunoglobulinsMaleMembrane ProteinsPhenotypeCodon, NonsenseIGSF1 protein, humanImmunoglobulinsMembrane ProteinsCentral hypothyroidismhypoprolactinemiaIGSF1

Identifiers

PMID32772515
PMCPMC8388056
OpenAlexW3048369480

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.